Canonical Allele Identifier: PA916027665
Gene: FCGR3A HGNC NCBI

Linked Data

ClinVar Variation Id: 156330
ClinVar RCV Id: RCV000455042
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316049.1:p.Ser65Asn
CA233189
NM_001329120.2:c.194G>A